HGVS | Genome Assembly |
---|---|
NC_000019.10:g.1103999T>A , CM000681.2:g.1103999T>A | GRCh38 |
NC_000019.9:g.1103998T>A , CM000681.1:g.1103998T>A | GRCh37 |
NC_000019.8:g.1054998T>A | NCBI36 |
NG_050621.1:g.5074T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706713.1:c.-45T>A | ENSP00000516510.1:n.-45T>A | |
ENST00000354171.13:c.-45T>A MANE Select | ENSP00000346103.7:n.-45T>A | |
ENST00000354171.12:c.-45T>A | ENSP00000346103.7:n.-45T>A | |
ENST00000616066.4:c.-45T>A | ENSP00000485000.1:n.-45T>A | |
NM_001039847.2:c.-45T>A | NP_001034936.1:n.-45T>A | |
NM_002085.4:c.-45T>A | NP_002076.2:n.-45T>A | |
NM_001039847.3:c.-45T>A | NP_001034936.1:n.-45T>A | |
NM_002085.5:c.-45T>A MANE Select | NP_002076.2:n.-45T>A |